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nsv7032846

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:379

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 16 studies. See in: genome view    
    Submitted genomic40,706,487-40,706,865Question Mark
    Overlapping variant regions from other studies: 114 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):39,335,127-39,335,505Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7032846Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2040,706,48740,706,865
    nsv7032846RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2039,335,12739,335,505

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18642869duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18642869Submitted genomicNC_000020.11:g.407
    06487_40706865dup
    GRCh38 (hg38)NC_000020.11Chr2040,706,48740,706,865
    nssv18642869RemappedPerfectNC_000020.10:g.393
    35127_39335505dup
    GRCh37.p13First PassNC_000020.10Chr2039,335,12739,335,505

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv186428694e-061244908
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